SDS Concentration Research Articles

Freezing and bioreactor in the low-concentration detergents: A novel approach in the decellularization of small-diameter arteries.

Using decellularized small-diameter vascular bypass substitutes (<6 mm) is an efficient method for bypass grafting. A solution containing 0.5% SDS (weight/volume) is commonly used for extended periods to generate acellular tissues. However, this solution causes damage to the microfibril structure and alters the mechanical forces. Hence, the objective of this study is to reduce the concentration of SDS to preserve the structure and achieve efficient decellularization. The study employs a diluted solution of 0.3% SDS (weight/volume) to treat fresh and frozen swine small-diameter arteries, utilizing physical methods such as freezing and thawing. The effectiveness of cell removal was evaluated using histological analysis and the remaining DNA content of the sample. Furthermore, the acellular circuit also assesses the cytotoxicity and proliferation of HUVECs to gauge their safety. Through the use of 0.3% SDS, a bioreactor system, and freezing-thawing, the pig arteries are successfully decellularized, resulting in residual DNA levels of less than 50 ng/mg dry weight. This process does not cause any major changes to the biomechanical or structural properties of the arteries. The acellular samples exhibit no toxicity on the L929 cell line and promote the growth of HUVECs at their highest rate on the fourth day. This allows for the placement of acellular vascular grafts to evaluate physiological processes within the animal body. This is an important requirement in clinical blood vessel transplantation.

Vascular decellularization dynamics: Optimizing Triton X-100 and SDS concentration with incubation time.

Vascular decellularization dynamics: Optimizing Triton X-100 and SDS concentration with incubation time.

Efficient decellularization of human fetal kidneys through optimized SDS exposure

Chronic kidney disease poses a significant threat to public health. Renal replacement therapy is the primary treatment option for end-stage kidney disease. However, there is a promising and relatively new method in regenerative medicine for creating a functional organ known as whole kidney decellularization. This method uses the intrinsic vasculature to perfuse the decellularizing agent into the tissue, effectively penetrating and removing cellular material. The regenerated bioscaffolds could serve as a source of organ donation. This study is focused on evaluating the effectiveness of various SDS exposures in decellularizing human fetal kidneys. The study included human fetal kidneys harvested from fetuses terminated before 14 weeks of gestational age. Kidneys were divided into six treatment groups based on SDS concentration and duration of perfusion. Decellularization, scanning electron microscopy, histopathological staining, immunofluorescent staining, and immunohistochemistry staining were performed to evaluate the adequacy of the process. The statistical analysis revealed that the SDS 0.1% treatment group had the highest collagen deposition after 24 h, significantly greater than the SDS 0.5% treatment group at 24 and 48 h. No significant differences were observed among the other treatment groups. The study concludes that the SDS 0.1% treatment group for 24 h was the most effective in terms of ECM content preservation and effective cell removal. This treatment showed better results than the other treatment groups and can be considered for future whole kidney decellularization studies.

Highly porous carbon with rich inherent groups for ultrahigh adsorption of organic dyes from wastewater

Activated carbon from renewable biomass or its waste to purify various dyeing wastewater from textile industry is highly desired. In this work, porous activated carbon was prepared by using silk waste as precursor via a simple one-step carbonization process. The obtained SWC-1-800 had ultrahigh adsorption for anionic dye AR73 and cationic dye MB owing to its ultrahigh specific surface area (2774 m2 g−1) and rich functional groups. SWC-1-800 had an increased adsorption capacity reaching 1310 and 928 mg g−1 for AR73 and MB respectively as the initial concentration up to 1000 mg L−1. Moreover, the adsorption capacity was stable under a wide range of Na+ and SDS concentration. By adjusting the temperature and pH value, the maximum adsorption capacity reached 1337 and 1000 mg g−1 for AR73 and MB respectively, keeping the removal rate of AR73 and MB more than 80 % after 5 adsorption cycles. Besides, SWC-1-800 demonstrated quite good adsorption ability for many other kinds of dyes, which adsorption capacity as high as 1998 mg g−1 (Rh B). The adsorption mechanism was further proposed according to the structural characteristics, inherent functional groups and adsorption properties. Using silk waste-derived carbon to effectively absorb the harmful dyes in the wastewater shows dual value for cleaner production via a “waste-waste to clean products” model, which has great application potential in dyeing wastewater purification.

Engineering the reverse micellar-templated Co(OH)2 nanospheres based Pickering emulsion and unveiling the mechanism of ambiguous phase separation

The present study employs reverse micellar-templated Co(OH)2 nanospheres, in situ hydrophobized with SDS in Pickering emulsion formulations and unlocking the mechanism of ambiguous phase separation at a certain surfactant concentration (4.3 mM). Co(OH)2 is synthesised in the core of reverse micelle: SPAN 80/1-butanol/water/toluene. Novel O/W Pickering emulsions have been developed with the help of positively charged (ς = 4.47 mV) Co(OH)2 (0.05 wt%) and an adequate amount of an anionic surfactant, SDS. An ambiguous phase separation of Pickering emulsion at 4.3 mM SDS is noticed within just 4 hr of standings, whereas, surprisingly stable O/W Pickering emulsions are found above and below these SDS concentrations. Upon addition of 2.6 mM SDS to the aqueous colloidal dispersion of Co(OH)2, the particles converted to amphiphilic one and stabilized the Pickering emulsion. However, these monolayer adsorbed surfactants face a hydrophobic interaction through tail-to-tail mode after adding 4.3 mM SDS to the colloidal dispersion. Consequently, they achieve a nanoplates-like architect and regain the extreme hydrophilic surface from both ends and eventually leads to the ambiguous phase separation through inter-droplet coalescence. The contact angle value altering from 44.9° (for 2.6 mM SDS) to 19.6° (for 4.3 mM SDS) confirms that the surface has changed from being amphiphilic to becoming extremely hydrophilic. Yet, again an increase in SDS (6.06 mM and onwards) suggest that surfactant molecules further adsorbed in either any of the two hydrophilic ends and revolving the particles to its previous amphiphilic state and eventually started to stabilise the emulsion droplets.

Pyranine Interaction with Amines in Micelles.

The fluorescence behavior of pyranine in anionic micellar system of sodium dodecyl sulphate was studied in the presence of selected amines. The amines included cyclopropylamine (CPA), ethylenediamine (EDA), benzylamine (BA), dibutylamine (DBA), cyclohexylamine (CHA), and polyethylenediamine (PEDA). All the studied amines quenched the intensity of pyranine. Study was performed in 0.05M and 0.1M SDS. The thermodynamic parameters were determined in order to understand the quenching of pyranine by the studied amines. Change in Gibbs free energy and quenching was found higher in 0.05M SDS concentration and was found lower when SDS concentration was increased to 0.1M SDS. Pyranine quenching by the amines studied were treated with an extended Stern-Volmer equation that produced the Stern-Volmer constant ([Formula: see text]). Binding constant (Kb), number of binding stoichiometry (n) and Gibbs free energy change (ΔGbinding) were found higher for lower surfactant concentration as compare to higher surfactant concentration. More negative (-ve) the Gibbs free energies more will be the quenching, higher will be the sensitivity and vice versa. The Gibbs free energies for all the studied amines were found in the order as cyclopropylamine > ethylenediamine > benzylamine > dibutylamine > cyclohexylamine > polyethylenediamine. Fluorescence quenching of pyranine by amines in aqueous SDS is reproducible and is useful for the determination of amines in environmental samples.

Influence of surfactants in nematic liquid crystal droplets

Liquid crystals in spherical droplets are highly sensitive to surfactants that control their orientation at interfaces. These molecules are widely used in optics. We fabricated 5CB liquid crystal droplets using SDS, CTAB, and DTAB surfactants at varying concentrations. We observed the transition from bipolar to radial at SDS concentration of 0.4 mM in 80 s, and from radial to bipolar at SDS concentration of 0.5 mM in 45 s. Surfactant concentration is the primary factor affecting liquid crystal droplet configuration, while headgroup, tail length, and architecture have minimal impact beyond the amount of absorbed surfactant in nematic liquid crystal droplets.

Surfactant Composition Dependent Evolution of Electronic/Structural Properties of P3HT Nanoparticle Colloids Synthesized via Mini-Emulsion Technique

: This study investigates the influence of surfactant (sodium dodecyl sulfate, SDS) concentration on the size and optoelectronic properties of poly(3-hexylthiophene) (P3HT) nanoparticles (NPs) synthesized via the mini-emulsion technique. P3HT NPs were fabricated with varying SDS concentrations. The size dependent optoelectronic properties, including the highest occupied molecular orbital (HOMO) and the lowest unoccupied molecular orbital (LUMO) levels, were analyzed through photoelectron spectroscopy in air, UV-Vis absorption spectroscopy and cyclic voltammetry. A clear trend of decreasing NP size with increasing SDS concentration was observed. Higher SDS levels resulted in smaller NPs with enhanced pi-pi stacking and shorter conjugation lengths. This structural change led to a noticeable shift in HOMO and LUMO levels, indicating a direct correlation between surfactant concentration and the electronic properties of the P3HT NPs. The absorption spectra revealed a decrease in the A0-0/A0-1 ratio with smaller NP size, suggesting a transition towards more pronounced H-aggregate characteristics. As the size of the P3HT NPs decreases, there is a notable increase in H-aggregate formation. This increase can be attributed to enhanced interchain interactions between the polymer chains. In smaller NPs, the surface area-to-volume ratio is higher, leading to more significant interactions between adjacent polymer chains. These interactions promote the formation of H-aggregates, characterized by their interchain pi-pi stacking, which differs from the intrachain coupling observed in J-aggregates.

Kinetic Study of Sodium Dodecylsulfate Degradation by Solar Heterogeneous Photocatalysis Based on Tungsten Oxide

Sodium Dodecyl Sulfate or SDS is a chemical compound widely used in detergent and cosmetic formulations. This work describes the application of solar heterogeneous photocatalysis based on tungsten oxide (WO3) to the kinetic study of the degradation of sodium dodecylsulfate. The experiments were performed at room temperature to study the effect of the initial catalyst mass. The results showed that a small amount of tungsten oxide is sufficient to degrade sodium dodecyl sulfate. The initial concentrations of SDS varied between 5 and 15 mg.L-1. According to the results, more than 87% reduction is obtained after 120 min of solar irradiation of the SDS solution for a WO3/SDS mass ratio of 1/5. The detailed kinetic analysis of the photodegradation of sodium dodecylsulfate showed that the disappearance of the anionic surfactant follows a pseudo-prime model. According to the Langmuir-Hinshelwood model, the kinetics constant calculated from the linear form of this model are : k = 0.042 mg.L.min-1 and K = 0.060 L.mg-1.

Nanoparticle-Mediated Plasmid Curing in Combating Antibiotic Resistance in Pathogenic Bacteria

Background: Nanotechnology has emerged as a pivotal domain in material science research with extensive applications across various sectors including biotechnology and medicine. Nanoparticles offer unique properties facilitating advancements in nanobiotechnology, particularly in nanomedicine, to combat bacterial infections and antibiotic resistance. This study aimed to determine the application of nanoparticles, specifically nano-TiO2, in treating plasmid-mediated antibiotic resistance in both Gram-negative and Gram-positive bacteria. Method: We evaluated antibiotic and nanomaterial sensitivity through disc diffusion and broth microdilution assays. Plasmid curing experiments were conducted using varying concentrations of nano-TiO2 and SDS as curing agents, followed by plasmid isolation and DNA extraction. The efficacy of nano-TiO2 in plasmid curing and DNA extraction was assessed, alongside the impact on bacterial growth and antibiotic resistance. Results: Results showed successful plasmid elimination with nano-TiO2 treatment, evidenced by the loss of plasmid DNA bands. Additionally, nano-TiO2 substantially enhanced DNA extraction efficiency and quality. The study indicated nano-TiO2's potential in combating antibiotic resistance by targeting plasmids, thereby presenting a novel approach in molecular biology techniques. Conclusion: In conclusion, this study underscores the promising role of nanoparticles in addressing bacterial infections and combating antibiotic resistance. Nano-TiO2 emerges as a valuable tool in DNA purification and plasmid curing, offering new avenues in molecular biology and antibiotic resistance research. However, further investigations are warranted to elucidate the broader implications of nanoparticles across diverse bacterial species and strains. These findings represent a significant step towards harnessing the potential of nanotechnology in combating antimicrobial resistance and advancing healthcare paradigms.

Pickering Emulsions of Thermotropic Liquid Crystals Stabilized by Amphiphilic Gold Nanoparticles.

We report emulsions of thermotropic liquid crystals (LCs) in water that are stabilized using amphiphilic gold nanoparticles (AuNPs) and retain their ability to respond to aqueous analytes for extended periods (e.g., up to 1 year after preparation). These LC emulsions exhibit exceptional colloidal stability that results from the adsorption of AuNPs that are functionalized with thiol-terminated poly(ethylene glycol) (PEG-thiol) and hexadecanethiol (C16-thiol) to LC droplet interfaces. These stabilized LC emulsions respond to the presence of model anionic (SDS), cationic (C12TAB), and nonionic (C12E4) surfactants in the surrounding aqueous media, as evidenced by ordering transitions in the LC droplets that can be readily observed using polarized light microscopy. Our results reveal significant differences in the sensitivity of the stabilized LC droplets toward each of these analytes. In particular, these stabilized droplets can detect the cationic C12TAB at concentrations that are lower than those required for bare LC droplets under similar experimental conditions (0.5 and 2 mM, respectively). These results demonstrate an enhanced sensitivity of the LC toward C12TAB when the PEG/C16-thiol-coated AuNPs are adsorbed at LC droplet interfaces. In contrast, the concentrations of SDS required to observe optical transformations in the stabilized LC droplets are higher than those required for the bare LC droplets, suggesting that the presence of the PEG/C16-thiol AuNPs reduces the sensitivity of the LC toward this analyte. When combined, our results show that this Pickering stabilization approach using amphiphilic AuNPs as stabilizing agents for LC-in-water emulsions provides a promising platform for developing LC droplet-based optical sensors with long-term colloidal stability as well as opportunities to tune the sensitivity and selectivity of the response to target aqueous analytes.

Effect of linear anionic surfactant (sodium dodecyl sulfate) dosage on nitrogen removal performance of an anammox reactor

AbstractThe impact of sodium dodecyl sulfate (SDS, as model linear anionic surfactant) dosage on overall nitrogen removal performance of anammox reactor alongside its microbial population and sludge properties was investigated. In this study (day 136), an anmmox sequencing batch biofilm reactor was subjected to gradual dosage of SDS from 0 to 20 mg L−1. Intriguingly, results revealed that SDS at ≥7.5 mg L−1 prompted sludge disintegration, evidenced by increased protein and polysaccharide content in the effluent. Nevertheless, reactor's average total nitrogen removal efficiency slightly improved from 83.12% (0 mg L−1) to 86.3% (20 mg L−1). The 16S rRNA gene sequencing revealed that SDS dosing significantly suppressed the unwanted and unavoidable nitrite oxidizing bacteria (NOBs) in the reactor as the abundance of genus Nitrospira declined from 40.68% (day 1) to 19.15% (day 136). The abundance of anammox genus Candidatus Kuenenia significantly improved from 1.86% (day 1) to 40.02% (day 136) as a result of NOB suppression. This study revealed that low concentration of surfactants in wastewater does not affect the anammox bacteria in a biofilm reactor. Furthermore, adding low concentrations of SDS (≥7.5 to 20 mg L−1) to wastewater may effectively suppress notorious NOBs in biofilm‐based anammox systems.

Effect of Five Different Antioxidants on the Effectiveness of Goat Semen Cryopreservation.

The effective combination of semen cryopreservation and artificial insemination has a positive effect on the conservation of germplasm resources, production and breeding, etc. However, during the process of semen cryopreservation, the sperm cells are very susceptible to different degrees of physical, chemical, and oxidative stress damage. Oxidative damage is the most important factor that reduces semen quality, which is affected by factors such as dilution equilibrium, change of osmotic pressure, cold shock, and enzyme action during the freezing-thawing process, which results in the aggregation of a large amount of reactive oxygen species (ROS) in sperm cells and affects the quality of semen after thawing. Therefore, the method of adding antioxidants to semen cryoprotective diluent is usually used to improve the effect of semen cryopreservation. The aim of this experiment was to investigate the effects of adding five antioxidants (GLP, Mito Q, NAC, SLS, and SDS) to semen cryoprotection diluent on the cryopreservation effect of semen from Saanen dairy goats. The optimal preservation concentrations were screened by detecting sperm viability, plasma membrane integrity, antioxidant capacity, and acrosomal enzyme activities after thawing, and the experimental results were as follows: the optimal concentrations of GLP, Mito Q, NAC, SLS, and SDS added to semen cryopreservation diluent at different concentrations were 0.8mg/mL, 150nmol/L, 0.6mg/mL, 0.15mg/ mL, 0.6mg/mL, and 0.15mg/mL. The optimal concentrations of the five antioxidants were added to the diluent and analyzed after 1week of cryopreservation, and it was found that sperm viability, plasma membrane integrity, and mitochondrial activity were significantly enhanced after thawing compared with the control group (P < 0.05), and their antioxidant capacity was significantly enhanced (P < 0.05). Therefore, the addition of the above five antioxidants to goat sperm cryodilution solution had a better enhancement of sperm cryopreservation. This study provides a useful reference for exploring the improvement of goat semen cryoprotection effect.

The role of adding nanoparticles and surfactant to the enzyme liquid binder in fluidized bed granulation process

The influence of enzyme liquid binder properties on wet granulation process was evaluated at both micro- and macro-scales. The micro-scale phenomena, including binder droplet spreading on and penetration into the powder bed, as well as liquid bridge shape and force, were analyzed by introducing SiO2 nanoparticles and SDS surfactant into the liquid binder containing a protease enzyme and 1 wt% of NaCMC. Moreover, the simultaneous effect of formulation variables, including NPs and SDS concentrations, and process conditions, such as binder spray rate and air temperature, was investigated using design of experiments. The average size and the span were considered as the responses. Nanofluid binder without SDS exhibited lower spreading and penetration times and a stronger bridge force. All formulation and process factors significantly influenced granule size distribution. Notably, increasing nanoparticle concentration and binder flow rate, while decreasing SDS concentration and air temperature, resulted in larger granules and a narrower size distribution.

AMWEst, a new thermostable and detergent-tolerant esterase retrieved from the Albian aquifer

A fosmid library was constructed with the metagenomic DNA from the high-temperature sediment-rich water of the Albian aquifer (Algeria). Functional screening of this library was subsequently done looking for genes encoding lipolytic enzymes. We identified a novel gene named AMWEst (1209 base pairs) encoding a protein of 402 amino acids with a predicted molecular weight of 43.44 kDa and conferring esterase activity. AMWEst was successfully overexpressed in the yeast mesophilic host Saccharomyces cerevisiae, and the expression system used proved to be efficient and produced sufficient activity for its biochemical characterization. Multiple sequence alignment indicated that AMWEst contained a conserved pentapeptide motif (Gly120-His121-Ser122-Gln123-Gly124). The optimum pH and temperature of the recombinant esterase AMWEst were 8 and 80 °C, respectively. Additionally, AMWEst showed higher activity towards short carbon substrates and showed maximum activity for p-nitrophenyl hexanoate (C6). Notably, AMWEst has a remarkable thermostability, and the enzyme retains almost maximum activity at 70 °C after incubation for 1 h. Moreover, enzyme activity was enhanced by high concentrations of SDS and Triton X-100 detergents.Key points• A novel thermostable esterase has been retrieved through functional metagenomics• The esterase is detergent-tolerant, which is attractive for some applications• The esterase can be expressed in a yeast mesophilic host to enhance its yield

The Early Endocytosis Gene PAL1 Contributes to Stress Tolerance and Hyphal Formation in Candida albicans.

The endocytic and secretory pathways of the fungal pathogen Candida albicans are fundamental to various key cellular processes such as cell growth, cell wall integrity, protein secretion, hyphal formation, and pathogenesis. Our previous studies focused on several candidate genes involved in early endocytosis, including ENT2 and END3, that play crucial roles in such processes. However, much remains to be discovered about other endocytosis-related genes and their contributions toward Candida albicans secretion and virulence. In this study, we examined the functions of the early endocytosis gene PAL1 using a reverse genetics approach based on CRISPR-Cas9-mediated gene deletion. Saccharomyces cerevisiae Pal1 is a protein in the early coat complex involved in clathrin-mediated endocytosis that is later internalized with the coat. The C. albicans pal1Δ/Δ null mutant demonstrated increased resistance to the antifungal agent caspofungin and the cell wall stressor Congo Red. In contrast, the null mutant was more sensitive to the antifungal drug fluconazole and low concentrations of SDS than the wild type (WT) and the re-integrant (KI). While pal1Δ/Δ can form hyphae and a biofilm, under some hyphal-inducing conditions, it was less able to demonstrate filamentous growth when compared to the WT and KI. The pal1Δ/Δ null mutant had no defect in clathrin-mediated endocytosis, and there were no changes in virulence-related processes compared to controls. Our results suggest that PAL1 has a role in susceptibility to antifungal agents, cell wall integrity, and membrane stability related to early endocytosis.

Synthesis of Calcium Carbonate Hollow Microspheres and the Pelletization Mechanism by Electrostatic Attraction of PEG-SDS.

Calcium carbonate is a common natural mineral with a wide range of applications. In this study, hollow calcite microspheres were successfully synthesized by using calcium chloride and sodium carbonate as raw materials in an SDS-PEG system. The results suggested that the appropriate concentration of SDS is necessary during the spherical crystallization of calcium carbonate. It was found that the crystals started to aggregate under the effect of SDS, and aggregation was enhanced with an increase in SDS concentration, leading to the transformation from hollow to solid microspheres. However, high temperatures will lead to the transformation from calcite to aragonite, resulting in the collapse of the formed spherical structure. Infrared spectroscopy and conductivity analysis suggested that when the concentration of SDS reached 0.3 g/L in the PEG-SDS system, SDS and PEG formed a spherical supramolecular structure. This structure could act as a template, leading to the aggregation of calcite through electrostatic attraction and finally to the formation of a hollow spherical structure.

Experimental study and prediction on the thermal management performance of SDS aqueous solution based microchannel flow boiling system

This study reports the flow boiling of SDS aqueous solution in straight and tree-shaped microchannel for thermal management. Under different volume flow rate and heat flux, the effect of SDS on the flow pattern, heat transfer and pressure drop in different channel structures is clarified. The results reflect that unique flow patterns like bubble stacking, bubble cluster and activated bubbles are observed in the flow boiling of SDS aqueous solution. 400 mg/kg and 200 mg/kg SDS aqueous solution has the best overall heat transfer enhancement performance in straight (25% improvement) and tree-shaped (22% improvement) microchannels respectively. The heat transfer enhancing mechanism of SDS can be summarized as suppressing the formation of large volume vapor slug and promote the rewetting of the bottom channel surface. Based on this mechanism, SDS can also advance the ONB and extend the stable nucleate boiling state, 100 mg/kg, and 400 mg/kg SDS aqueous solution show longest stable nucleate boiling state in straight and tree-shaped microchannel respectively. Increasing solute concentration of SDS leads to larger pressure drop and stronger pressure drop fluctuation in both microchannels, but increasing volume flow rate will suppress this extra resistance and instability caused by SDS. Targeted heat transfer and pressure drop correlations are also presented.

Study on the Remediation of Pyrene-Contaminated Soil with Surfactants and their Mechanisms

Soil is the main aggregation site of polycyclic aromatic hydrocarbons and an important pathway of migration to other media. In this paper, the adsorption behavior of pyrene and seven different types of surfactants on kaolinite surfaces was studied by molecular dynamics simulation and desorption testing. The molecular dynamics simulation results showed that pyrene was more easily adsorbed on the 001 (-) side of kaolinite. SDBS, SDS, TW80, and TX-100 had strong interactions with pyrene, encapsulating pyrene molecules in aggregates. However, when the concentration of surfactant was too high, the desorption of pyrene molecules on a kaolinite surface will be inhibited. The desorption of pyrene molecules will be inhibited in the presence of BS-12, TW80, and TX-100, while the desorption process can be promoted by using CTAC, DDBAC, SDBS, and SDS as soil remediation agents. The removal rate of pyrene gradually increased with the increase of SDS dosage, while for SDBS, the removal rate showed a trend of first increasing and then decreasing. When the concentration of SDS was 0.014 mol/L, the elution rate of pyrene reached 72.86%. The molecular dynamics simulation results were similar to the desorption test results, verifying the reliability of molecular dynamics simulation. The research results provide theoretical support for the selection of surfactants in the remediation process of pyrene-contaminated soil.

Perturbation of surfactant-induced amyloids by abolishing electrostatic interactions

Protein amyloid fibrils are supramolecular homopolymers that play a role in numerous biological processes and illnesses. The link between type 2 diabetes and insulin-induced amyloidosis has prompted much research on the production of insulin amyloid fibrils. Many in vitro investigations have shown that insulin can turn into amyloid fibrils under certain conditions. Insulin was used as a model protein in this study to determine the role of electrostatic interactions in surfactant-induced amyloids. Our results showed that SDS-induced amyloid formation was nucleation-independent at pH 2.0, and the solubilization was also instantaneous upon electrostatic interaction disruption. Far UV circular dichroism (CD), turbidity, Rayleigh light scattering (RLS), thioflavin T (ThT), and transmission electron microscopy (TEM) imaging showed the attainment of the different structural forms of insulin due to varying degrees of electrostatic interactions between the anionic surfactant (SDS) and the cationic to the anionic state of insulin. Treatment of SDS with the cationic state of insulin strongly induces amyloid-like aggregate while anionic state insulin reverts to native-like alpha-helical structures. In all samples, SDS concentration remained unchanged. Thus, hydrophobicity remained constant; only the electrostatic interaction between anionic SDS and cationic insulin was abolished as pH increased.